A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111703



Internal ID21294969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:139110848..139180867hg38UCSC Ensembl
InnerchrX:138193010..138263029hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3870020
hg1970020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105097
Samplessample240
Known GenesFGF13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111703
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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